Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18030 | A09 | 10806626 | C | T | missense_variant | MODERATE | c.1391C>T|p.Ala464Val |
S293 |